Skip to content

NovoTHOR XL 3.0Recalls & reported problems

Thor Photomedicine Limited · S2190 NovoTHOR XL · Class 2

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jul 24, 2025Open, Classified

    The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

    Z-2417-2025 · Root cause: Process control · FDA record ↗

  2. Nov 20, 2023Open, Classified

    One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy

    Z-0972-2024 · Root cause: Component design/selection · FDA record ↗

Other Lamp, Infrared, Therapeutic Heating devices

All Lamp, Infrared, Therapeutic Heating devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.